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Horrific and Deadly Effects of Antidepressants

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11 minute read

 The Vigilant Fox

Once you see what else these drugs are doing, you’ll never look at depression “treatment” the same way again.

The following information is based on a report originally published by A Midwestern Doctor. Key details have been streamlined and editorialized for clarity and impact. Read the original report here.

Did you know that SSRI antidepressants INCREASE suicidal thoughts by 255%?

A clinical trial on healthy volunteers found that 2 out of 20 became suicidal after taking Zoloft.

One was literally on her way to kill herself when a timely phone call saved her life.

But it’s not just suicidal thoughts that make antidepressants dangerous.

And once you see what else these drugs are doing, you’ll never look at depression “treatment” the same way again.

Selective serotonin reuptake inhibitors—or SSRIs—are one of the most harmful medicines prescribed today.

And that’s saying a lot because the market is FULL of harmful medicines.

What’s so bad about these antidepressants?

First of all, their use is widespread and frequently unjustifiable.

They promise to be a magical solution to depression and anxiety, but it’s quite the opposite.

In fact, they can cause side effects far worse than what they claim to treat.

SSRIs don’t just dull your emotions, and they don’t alter your brain chemistry for the better.

They literally reprogram your brain.

Between 40% and 60% of users report emotional numbness. Not just negative emotions—all emotions.

Joy, pain, motivation—all of it completely flatlined.

Some describe it as “life without color” or a “zombie-like” existence.

Sure, maybe you don’t feel depressed anymore. But you don’t feel anything at all.

That sounds… terrible.

Depression can be serious, but should we accept emotionless zombies as the alternative?

If you want to dig even deeper into the dark side of antidepressants and why they’re so harmful, check out @Midwesterndoc’s comprehensive report on the subject. And be sure to share this with anyone you know who may be considering starting an SSRI.

And it’s not just becoming an emotionless zombie you have to worry about. The emotional shutdown can lead to something that is much worse than depression and anxiety.

Psychotic violence.

I don’t mean just a little anger here and there.

SSRIs are causing people to commit suicide—and yes, even horrific mass shootings.

And guess what? The FDA knew about it.

Prozac triggers hallucinations, mania, and violence, and the FDA has known all along.

Even animals become aggressive on SSRIs.

But instead of going back to the drawing board, the FDA approved it anyway.

After nine years on the market, 39,000 people reported major psychiatric events. And those are only the people who reported it…

Really makes you question FDA approval, doesn’t it?

Did you know most of the mass shooters we hear about in the news were often on SSRIs?

It’s true.

And the media even reported on it. But then, they stopped.

That’s weird.

So why are we “not allowed” to talk about SSRIs and violence anymore?

It’s pretty simple.

It would blow the lid off one of the most dangerous pharmaceutical cover-ups in modern history.

It would expose the truth that Big Pharma knowingly released drugs that could make people snap and kill other people.

And they just kept selling them anyway.

But the psychotic violence caused by SSRIs is only the tip of the iceberg.

Obviously, not everyone taking these drugs becomes a mass shooter. But that doesn’t mean the other side effects are any less terrible for those who experience them.

SSRIs truly warp your mind, body, and emotions. And sometimes it is irreversible.

The numbers are truly chilling:
→ A 255% increase in suicidal thoughts
→ 30% of SSRI users develop Bipolar disorder
→ 59% suffer long-term sexual dysfunction

With many saying their libido never came back even after stopping the drug.

The science is clear. The harm caused by SSRIs greatly outweighs any benefits they provide.

Talk about depressing…

A 2020 study involving 20 healthy volunteers with zero history of depression or other mental illnesses had shocking results.

They were each given Zoloft.

TWO of them BECAME suicidal.

One of them was even on her way to kill herself when a divinely timed phone call interrupted her plans.

These two study participants were still affected several months later. They were actually questioning the stability of their personalities.

This doesn’t sound like a magic solution. This sounds like torture.

Speaking of stopping SSRIs—good luck!

They are highly addictive.

And it’s not just physical addiction. It’s neurological.

And because of what they do to the brain, it can take years to step down the dose and wean off of them. Years!

Withdrawal symptoms include things like:
– Brain zaps
– Panic attacks
– Suicidal spirals
– Derealization

And these symptoms can last weeks, months, or even years.

It’s not uncommon to fail and continue taking them because the withdrawal is just that bad.

A 2022 review found that 56% of users who tried to stop SSRIs experience withdrawal symptoms, and 46% describe it as severe.

Psychiatrists mislabel it as a “relapse” and prescribe even more drugs.

The system is set up to trap you. There’s no exit.

And the most vulnerable groups?

Pregnant women and children.

Despite strong evidence linking SSRIs to birth defects, premature birth, and newborn deaththe FDA still endorses their use during pregnancy.

One study showed a six times higher risk of pulmonary hypertension in newborns.

Another study showed that SSRI babies lost height and weight in just 19 weeks.

This isn’t good.

SSRIs are being pushed on everyone. Especially vulnerable people like foster kids, parolees, prisoners, and elderly nursing home residents.

And in many of these cases, there is no real ability for them to say no.

That’s not mental health care. That’s drugging people.

The industry tells us SSRIs are “fixing a serotonin imbalance.”

But that’s a lie.

There’s no solid evidence that depression is caused by low serotonin.

So what’s the real mechanism at play here?

SSRIs alter brain wiring. And obviously not always in good ways.

SSRI users describe feeling like their “personality changed” after starting the drug.

The reports are endless and absolutely chilling.

Some were left numb for years. Others became aggressive, impulsive, or dissociated from reality.

Many say they don’t recognize who they became after taking SSRIs.

Excuse me… what?!

And of course, patients and their families are rarely warned about these effects.

Most say they were never told about the risks. There was no informed consent.

How can you not inform depressed people that their medication might make them suicidal? How is it even possible that we can be asking that question?

They experienced these things and talked to their doctors.

They were gaslit every step of the way.

If you or someone you love is taking SSRIs or is considering taking them, I urge you to read the full report from A Midwestern Doctor

How many more people have to suffer before this ends?

How many more people who reach out to their doctor because something is off and they’re looking for help are going to be hurt, sometimes permanently?

It’s time to expose the cover-up and end Big Pharma’s abuse and gaslighting once and for all.

RFK Jr. is right—this could finally be the turning point.

For 40 years, this tragedy was hidden behind slick ads and corrupted science.

But now it’s in the light and MAHA is ready to fight.

If you know anyone considering starting an SSRI, be sure to forward them this information. Because if you wait until after, it might be too late.

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Thanks for reading!

This information was based on a report originally published by A Midwestern Doctor. Key details were streamlined and editorialized for clarity and impact. 

Read the original report here.

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Daily Caller EXCLUSIVE: Trump’s Broad Ban On Risky Gain-Of-Function Research Nears Completion

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From the Daily Caller News Foundation

By Emily Kopp

President Donald Trump could sign a sweeping executive order banning gain-of-function research — research that makes viruses more dangerous in the lab — as soon as May 6, according to a source who has worked with the National Security Council on the issue.

The executive order will take a broad strokes approach, banning research amplifying the infectivity or pathogenicity of any virulent and replicable pathogen, according to the source, who requested anonymity to speak candidly about the anticipated executive action. But significant unresolved issues remain, according to the source, including whether violators will be subject to criminal penalties as bioweaponeers.

The executive order is being steered by Gerald Parker, head of the White House Office of Pandemic Preparedness and Response Policy, which has been incorporated into the NSC. Parker did not respond to requests for comment.

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In the process of drafting the executive order, Parker has frozen out the federal agencies that have for years championed gain-of-function research and staved off regulation — chiefly Anthony Fauci’s former institute, the National Institute of Allergy and Infectious Diseases at the National Institutes of Health.

The latest policy guidance on gain-of-function research, unveiled under the Biden administration in 2024, was previously expected to go into effect May 6. According to a March 25 letter cosigned by the American Society for Microbiology, the Association for Biosafety and Biosecurity International, and Council on Governmental Relations, organizations that conduct pathogen research have not received direction from the NIH on that guidance — suggesting the executive order would supersede the May 6 deadline.

The 2024 guidance altered the scope of experiments subject to more rigorous review, but charged researchers, universities and funding agencies like NIH with its implementation, which critics say disincentivizes reporting. Many scientists say that researchers and NIH should not be the primary entities conducting cost–benefit analyses of pandemic virus studies. 

Parker previously served as the head of the National Science Advisory Board for Biosecurity (NSABB), a group of outside experts that advises NIH on biosecurity matters, and in that role recommended that Congress stand up a new government agency to advise on gain-of-function research. Former Centers for Disease Control and Prevention Director Robert Redfield has also endorsed moving gain-of-function research decision making out of the NIH to an independent commission.

“Given the well documented lapses in the NIH review process, policymakers should … remove final approval of any gain-of function research grants from NIH,” Redfield said in a February op-ed.

It remains to be seen whether the executive order will articulate carveouts for gain-of-function research without risks of harm such as research on non-replicative pseudoviruses, which can be used to study viral evolution without generating pandemic viruses.

It also remains to be seen whether the executive order will define “gain-of-function research” tightly enough to stand up to legal scrutiny should a violator be charged with a crime.

Risky research on coronaviruses funded by the NIH at the Wuhan Institute of Virology through the U.S. nonprofit EcoHealth Alliance typifies the loopholes in NIH’s existing regulatory framework, some biosecurity experts say.

Documents obtained through the Freedom of Information Act in 2023 indicated that EcoHealth Alliance President Peter Daszak submitted a proposal to the Pentagon in 2018 called “DEFUSE” describing gain-of-function experiments on viruses similar to SARS-CoV-2 but downplayed to his intended funder the fact that many of the tests would occur in Wuhan, China.

Daszak and EcoHealth were both debarred from federal funding in January 2025 but have faced no criminal charges.

“I don’t know that criminal penalties are necessary. But we do need more sticks in biosafety as well as carrots,” said a biosecurity expert who requested anonymity to avoid retribution from his employer for weighing in on the expected policy. “For instance, biosafety should be a part of tenure review and whether you get funding for future work.”

Some experts say that it is likely that the COVID-19 crisis was a lab-generated pandemic, and that without major policy changes it might not be the last one.

“Gain-of-function research on potential pandemic pathogens caused the COVID-19 pandemic, killing 20 million and costing $25 trillion,” said Richard Ebright, a Rutgers University microbiologist and longtime critic of high-risk virology, to the Daily Caller News Foundation. “If not stopped, gain-of-function research on potential pandemic pathogens likely will cause future lab-generated pandemics.”

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WHO member states agree on draft of ‘pandemic treaty’ that could be adopted in May

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From LifeSiteNews

By Andreas Wailzer

The WHO draft ‘pandemic accord’ includes data sharing between governments and pharmaceutical companies to develop ‘pandemic-related health products,’ though it would not apply to the US.

Representatives of WHO member states have agreed on a draft of the “pandemic accord” that is scheduled to be voted on next month.

“The nations of the world made history in Geneva today,” Dr. Tedros Adhanom Ghebreyesus, Director-General of the WHO, said after the member states agreed on the draft of the pandemic treaty on Wednesday.

“In reaching consensus on the Pandemic Agreement, not only did they put in place a generational accord to make the world safer, they have also demonstrated that multilateralism is alive and well, and that in our divided world, nations can still work together to find common ground, and a shared response to shared threats. I thank WHO’s Member States, and their negotiating teams, for their foresight, commitment and tireless work. We look forward to the World Health Assembly’s consideration of the agreement and – we hope – its adoption,” the WHO leader continued.

The agreement was reached by the Intergovernmental Negotiating Body (INB), the committee set up by the WHO to negotiate the treaty, after more than three years of negotiations.

According to the WHO’s press release, the core pandemic treaty draft includes the establishment of “a pathogen access and benefit sharing system,” allowing the sharing of data between governments and pharmaceutical companies aimed at quickly developing and supplying “pandemic-related health products” during a pandemic. These “health products” could be dangerous mRNA injections, similar to those rolled out and imposed on large parts of the world population during the COVID-19 crisis.

The WHO claims that the “proposal affirms the sovereignty of countries to address public health matters within their borders, and provides that nothing in the draft agreement shall be interpreted as providing WHO any authority to direct, order, alter or prescribe national laws or policies, or mandate States to take specific actions, such as ban or accept travellers, impose vaccination mandates or therapeutic or diagnostic measures or implement lockdowns.”

The WHO seems to be responding to critics of the Pandemic Treaty, who have argued it is a power grab by the WHO. It would give the global organization unchecked power whenever it declares that any health risk is a “pandemic.” However, the new draft has not yet been made public, making a thorough assessment impossible.

WHO director-general Ghebreyesus engaged in his typical fear-mongering, stating, “Virus is the worst enemy. (It) could be worse than a war.”

READ: WHO director Tedros calls for ‘more aggressive’ action against COVID shot critics

While the WHO pandemic treaty and the amendments to the International Health Regulations (IHR) failed to pass last year, the new version of the agreement could be passed by a two-thirds majority at the annual World Health Assembly (May 19-27, 2025) next month.

However, the U.S. was not part of the negotiations and would not be bound by the agreement since President Donald Trump withdrew the country from the international body in January 2025 after taking office for his second term. Argentine President Javier Milei announced in February that his country will also leave the WHO, following Trump’s example. If more countries were to leave the WHO, the pandemic agreement could be ineffective in practice, even if it were to pass in May.

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